Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264836Generated: November 1, 2026

Hydrochloric Acid → 4-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran

https://huagongshe.com/reaction/264836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant2,2-bisfluoromethyl-3,4-dihydro-6-nitro-2H-1-benzopyran-4-oneHCID 15545853—
Catalystzinc(II)iodideHCID 9883512—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
Product4-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyranHCID 21194980—

Reaction Steps

To a mixture of 4.05 g of 2,2-bis(fluoromethyl)-3,4-dihydro-6-nitro-2H-1-benzopyran-4-one and 10 ml of dried benzene was added 2.52 ml of trimethylsilyl cyanide with stirring under ice-cooling. 0.82 g of zinc iodide was added therein and the mixture was stirred at room temperature for 12 hours. Further, 8 ml of pyridine and 4.41 ml of phosphorus oxychloride were added therein and the resultant mixture was refluxed with heating for 6 hours. Ice water was added to the residue and it was acidified to be hydrochloric acid and it was extracted with methylene chloride. An organic layer was washed with water and dried, and the solvent was distilled. The obtained residue was purified according to silica gel column chromatography (developing solution, CH2Cl2 :hexane=7:3) to obtain 0.99 g of 4-cyano-2,2-bis(fluoromethyl)-6-nitro-2H-1-benzopyran with a melting point of 136°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646308
Source datasetuspto-grants-1997_07
ORD IDord-07154dedc489443eb097a9500e574f78
Source noteuspto-grants-1997_07